Trials / Completed
CompletedNCT00858715
Resistance to Antithrombotic Therapy
Resistance to Antithrombotic Therapy in Patients Undergoing Angioplasty and Stenting for Cardiovascular Disease - Vienna REACT
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 46 (actual)
- Sponsor
- Medical University of Vienna · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Clopidogrel plays a pivotal role in the antithrombotic regimen after percutaneous intervention with stent implantation. However, response to clopidogrel shows a wide interindividual variability and a high on-treatment residual ADP-inducible platelet reactivity has already been associated with an increased risk for adverse events after coronary stenting. In the present study, platelet reactivity will be determined by 6 different platelet function tests in patients on dual antiplatelet therapy after angioplasty and stenting for peripheral, coronary and carotid artery disease. One hundred patients showing high on-treatment residual ADP-inducible platelet reactivity in 2 or more tests will be randomized to receive either 75mg or 150mg of daily clopidogrel in addition to aspirin for 3 months. The aim of the present study is to investigate the effects of intensified antithrombotic therapy (150mg clopidogrel + 100mg aspirin daily) versus standard antithrombotic therapy (75mg clopidogrel + 100mg aspirin daily) in patients with decreased clopidogrel-mediated platelet inhibition after percutaneous intervention with stent implantation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | aspirin | 100 mg aspirin |
| DRUG | clopidogrel | 75 mg (Arm 1) and 150 mg (Arm 2) |
Timeline
- Start date
- 2008-05-01
- Primary completion
- 2012-05-01
- Completion
- 2012-05-01
- First posted
- 2009-03-10
- Last updated
- 2012-12-12
Locations
1 site across 1 country: Austria
Source: ClinicalTrials.gov record NCT00858715. Inclusion in this directory is not an endorsement.